A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140927



Internal ID19259126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:109181277..109181344hg38UCSC Ensembl
Outerchr8:110193506..110193573hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992435
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140927
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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